A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981303



Internal ID12973140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19961836..22288239hg38UCSC Ensembl
Innerchr15:20167089..22576190hg19UCSC Ensembl
Innerchr15:18427103..20077554hg18UCSC Ensembl
Innerchr15:18427103..20077554hg17UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382326404
hg192409102
hg181650452
hg171650452
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35036
Supporting Variants
SamplesBEC_382
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2, REREP3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981303
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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